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Gene expression and DNA methylation are extensively coordinated with MRI-based brain microstructural characteristics
Cognitive function relies on both molecular levels and cellular structures. However, systematic relationships between these two components of cognitive function, and their joint contribution to disease, are largely unknown. We utilize postmortem neuroimaging in tandem with gene expression and DNA me...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6309607/ https://www.ncbi.nlm.nih.gov/pubmed/29934819 http://dx.doi.org/10.1007/s11682-018-9910-4 |
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author | Gaiteri, Chris Dawe, Robert Mostafavi, Sara Blizinsky, Katherine D. Tasaki, Shinya Komashko, Vitalina Yu, Lei Wang, Yanling Schneider, Julie A. Arfanakis, Konstantinos De Jager, Philip L. Bennett, David A. |
author_facet | Gaiteri, Chris Dawe, Robert Mostafavi, Sara Blizinsky, Katherine D. Tasaki, Shinya Komashko, Vitalina Yu, Lei Wang, Yanling Schneider, Julie A. Arfanakis, Konstantinos De Jager, Philip L. Bennett, David A. |
author_sort | Gaiteri, Chris |
collection | PubMed |
description | Cognitive function relies on both molecular levels and cellular structures. However, systematic relationships between these two components of cognitive function, and their joint contribution to disease, are largely unknown. We utilize postmortem neuroimaging in tandem with gene expression and DNA methylation, from 222 deeply-phenotyped persons in a longitudinal aging cohort. Expression of hundreds of genes and methylation at thousands of loci are related to the microstructure of extensive regions of this same set of brains, as assessed by MRI. The genes linked to brain microstructure perform functions related to cell motility, transcriptional regulation and nuclear processes, and are selectively associated with Alzheimer’s phenotypes. Similar methodology can be applied to other diseases to identify their joint molecular and structural basis, or to infer molecular levels in the brain on the basis of neuroimaging for precision medicine applications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11682-018-9910-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6309607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-63096072019-08-06 Gene expression and DNA methylation are extensively coordinated with MRI-based brain microstructural characteristics Gaiteri, Chris Dawe, Robert Mostafavi, Sara Blizinsky, Katherine D. Tasaki, Shinya Komashko, Vitalina Yu, Lei Wang, Yanling Schneider, Julie A. Arfanakis, Konstantinos De Jager, Philip L. Bennett, David A. Brain Imaging Behav Original Research Cognitive function relies on both molecular levels and cellular structures. However, systematic relationships between these two components of cognitive function, and their joint contribution to disease, are largely unknown. We utilize postmortem neuroimaging in tandem with gene expression and DNA methylation, from 222 deeply-phenotyped persons in a longitudinal aging cohort. Expression of hundreds of genes and methylation at thousands of loci are related to the microstructure of extensive regions of this same set of brains, as assessed by MRI. The genes linked to brain microstructure perform functions related to cell motility, transcriptional regulation and nuclear processes, and are selectively associated with Alzheimer’s phenotypes. Similar methodology can be applied to other diseases to identify their joint molecular and structural basis, or to infer molecular levels in the brain on the basis of neuroimaging for precision medicine applications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11682-018-9910-4) contains supplementary material, which is available to authorized users. Springer US 2018-06-22 2019 /pmc/articles/PMC6309607/ /pubmed/29934819 http://dx.doi.org/10.1007/s11682-018-9910-4 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Gaiteri, Chris Dawe, Robert Mostafavi, Sara Blizinsky, Katherine D. Tasaki, Shinya Komashko, Vitalina Yu, Lei Wang, Yanling Schneider, Julie A. Arfanakis, Konstantinos De Jager, Philip L. Bennett, David A. Gene expression and DNA methylation are extensively coordinated with MRI-based brain microstructural characteristics |
title | Gene expression and DNA methylation are extensively coordinated with MRI-based brain microstructural characteristics |
title_full | Gene expression and DNA methylation are extensively coordinated with MRI-based brain microstructural characteristics |
title_fullStr | Gene expression and DNA methylation are extensively coordinated with MRI-based brain microstructural characteristics |
title_full_unstemmed | Gene expression and DNA methylation are extensively coordinated with MRI-based brain microstructural characteristics |
title_short | Gene expression and DNA methylation are extensively coordinated with MRI-based brain microstructural characteristics |
title_sort | gene expression and dna methylation are extensively coordinated with mri-based brain microstructural characteristics |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6309607/ https://www.ncbi.nlm.nih.gov/pubmed/29934819 http://dx.doi.org/10.1007/s11682-018-9910-4 |
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